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FAMILY CARE ULTRA STRENGTH PAIN RELIEF
FAMILY CARE ULTRA STRENGTH PAIN RELIEF - 65923-008-32 - (CAMPHOR, MENTHOL)
Drug Information of FAMILY CARE ULTRA STRENGTH PAIN RELIEF
| Product NDC: | 65923-008 |
| Proprietary Name: | FAMILY CARE ULTRA STRENGTH PAIN RELIEF |
| Non Proprietary Name: | CAMPHOR, MENTHOL |
| Active Ingredient(s): | 110; 110 mg/g; mg/g & nbsp; CAMPHOR, MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FAMILY CARE ULTRA STRENGTH PAIN RELIEF
| Product NDC: | 65923-008 |
| Labeler Name: | UNITED EXCHANGE CORP. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120214 |
Package Information of FAMILY CARE ULTRA STRENGTH PAIN RELIEF
| Package NDC: | 65923-008-32 |
| Package Description: | 1 JAR in 1 CARTON (65923-008-32) > 8 g in 1 JAR |
NDC Information of FAMILY CARE ULTRA STRENGTH PAIN RELIEF
| NDC Code | 65923-008-32 |
| Proprietary Name | FAMILY CARE ULTRA STRENGTH PAIN RELIEF |
| Package Description | 1 JAR in 1 CARTON (65923-008-32) > 8 g in 1 JAR |
| Product NDC | 65923-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR, MENTHOL |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120214 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | UNITED EXCHANGE CORP. |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
| Strength Number | 110; 110 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
